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α-MSH tripeptide analogs activate the melanocortin 1 receptor and reduce UV-induced DNA damage in human melanocytes

✍ Scribed by Zalfa A. Abdel-Malek; Andrew Ruwe; Renny Kavanagh-Starner; Ana Luisa Kadekaro; Viki Swope; Carrie Haskell-Luevano; Leonid Koikov; James J. Knittel

Book ID
118074722
Publisher
Wiley (Blackwell Publishing)
Year
2009
Tongue
English
Weight
365 KB
Volume
22
Category
Article
ISSN
1755-1471

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## Abstract α‐Melanocyte stimulating hormone (αMSH), Ac‐Ser^1^‐Tyr^2^‐Ser^3^‐Met^4^‐Glu^5^‐His^6^‐Phe^7^‐Arg^8^‐Trp^9^‐Gly^10^‐Lys^11^‐Pro^12^‐Val^13^‐NH~2~, is an endogenous agonist for the melanocortin receptor 1 (MC1R), the receptor found in the skin, several types of immune cells, and other per